Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm
Abdominal aortic aneurysm (AAA) was previously ascribed to weaken defective medial arterial/adventitial layers, for example, smooth muscle/fibroblast cells. Therefore, besides surgical repair, medications targeting the medial layer to strengthen the aortic wall are the most feasible treatment strate...
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doaj-74a1c21ac8df4aecba4bd885dd76c15a2020-11-24T21:23:38ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942018-01-01201810.1155/2018/63065426306542Endothelium as a Potential Target for Treatment of Abdominal Aortic AneurysmJingyuan Sun0Hongping Deng1Zhen Zhou2Xiaoxing Xiong3Ling Gao4Endocrinology & Metabolism Department, Renmin Hospital of Wuhan University, Wuhan, ChinaVascular Surgery Department, Renmin Hospital of Wuhan University, Wuhan, ChinaVascular Surgery Department, Renmin Hospital of Wuhan University, Wuhan, ChinaNeurosurgery Department, Renmin Hospital of Wuhan University, Wuhan, ChinaEndocrinology & Metabolism Department, Renmin Hospital of Wuhan University, Wuhan, ChinaAbdominal aortic aneurysm (AAA) was previously ascribed to weaken defective medial arterial/adventitial layers, for example, smooth muscle/fibroblast cells. Therefore, besides surgical repair, medications targeting the medial layer to strengthen the aortic wall are the most feasible treatment strategy for AAA. However, so far, it is unclear whether such drugs have any beneficial effect on AAA prognosis, rate of aneurysm growth, rupture, or survival. Notably, clinical studies have shown that AAA is highly associated with endothelial dysfunction in the aged population. Additionally, animal models of endothelial dysfunction and endothelial nitric oxide synthase (eNOS) uncoupling had a very high rate of AAA formation, indicating there is crucial involvement of the endothelium and a possible pharmacological solution targeting the endothelium in AAA treatment. Endothelial cells have been found to trigger vascular wall remodeling by releasing proteases, or recruiting macrophages along with other neutrophils, into the medial layer. Moreover, inflammation and oxidative stress of the arterial wall were induced by endothelial dysfunction. Interestingly, there is a paradoxical differential correlation between diabetes and aneurysm formation in retinal capillaries and the aorta. Deciphering the significance of such a difference may explain current unsuccessful AAA medications and offer a solution to this treatment challenge. It is now believed that AAA and atherosclerosis are two separate but related diseases, based on their different clinical patterns which have further complicated the puzzle. Therefore, a thorough investigation of the interaction between endothelium and medial/adventitial layer may provide us a better understanding and new perspective on AAA formation, especially after taking into account the importance of endothelium in the development of AAA. Moreover, a novel medication strategy replacing the currently used, but suboptimal treatments for AAA, could be informed with this analysis.http://dx.doi.org/10.1155/2018/6306542 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jingyuan Sun Hongping Deng Zhen Zhou Xiaoxing Xiong Ling Gao |
spellingShingle |
Jingyuan Sun Hongping Deng Zhen Zhou Xiaoxing Xiong Ling Gao Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm Oxidative Medicine and Cellular Longevity |
author_facet |
Jingyuan Sun Hongping Deng Zhen Zhou Xiaoxing Xiong Ling Gao |
author_sort |
Jingyuan Sun |
title |
Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm |
title_short |
Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm |
title_full |
Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm |
title_fullStr |
Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm |
title_full_unstemmed |
Endothelium as a Potential Target for Treatment of Abdominal Aortic Aneurysm |
title_sort |
endothelium as a potential target for treatment of abdominal aortic aneurysm |
publisher |
Hindawi Limited |
series |
Oxidative Medicine and Cellular Longevity |
issn |
1942-0900 1942-0994 |
publishDate |
2018-01-01 |
description |
Abdominal aortic aneurysm (AAA) was previously ascribed to weaken defective medial arterial/adventitial layers, for example, smooth muscle/fibroblast cells. Therefore, besides surgical repair, medications targeting the medial layer to strengthen the aortic wall are the most feasible treatment strategy for AAA. However, so far, it is unclear whether such drugs have any beneficial effect on AAA prognosis, rate of aneurysm growth, rupture, or survival. Notably, clinical studies have shown that AAA is highly associated with endothelial dysfunction in the aged population. Additionally, animal models of endothelial dysfunction and endothelial nitric oxide synthase (eNOS) uncoupling had a very high rate of AAA formation, indicating there is crucial involvement of the endothelium and a possible pharmacological solution targeting the endothelium in AAA treatment. Endothelial cells have been found to trigger vascular wall remodeling by releasing proteases, or recruiting macrophages along with other neutrophils, into the medial layer. Moreover, inflammation and oxidative stress of the arterial wall were induced by endothelial dysfunction. Interestingly, there is a paradoxical differential correlation between diabetes and aneurysm formation in retinal capillaries and the aorta. Deciphering the significance of such a difference may explain current unsuccessful AAA medications and offer a solution to this treatment challenge. It is now believed that AAA and atherosclerosis are two separate but related diseases, based on their different clinical patterns which have further complicated the puzzle. Therefore, a thorough investigation of the interaction between endothelium and medial/adventitial layer may provide us a better understanding and new perspective on AAA formation, especially after taking into account the importance of endothelium in the development of AAA. Moreover, a novel medication strategy replacing the currently used, but suboptimal treatments for AAA, could be informed with this analysis. |
url |
http://dx.doi.org/10.1155/2018/6306542 |
work_keys_str_mv |
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